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SEC23IP encodes a member of the phosphatidic acid preferring-phospholipase A1 family. Additionally we are shipping SEC23 Interacting Protein Proteins (4) and SEC23 Interacting Protein Kits (2) and many more products for this protein.
Showing 10 out of 44 products:
Human Polyclonal SEC23IP Primary Antibody for WB - ABIN658432
Klinkenberg, Long, Shome, Watkins, Aridor: A cascade of ER exit site assembly that is regulated by p125A and lipid signals. in Journal of cell science 2014
Human Polyclonal SEC23IP Primary Antibody for ICC, IF - ABIN4352403
Stadler, Rexhepaj, Singan, Murphy, Pepperkok, Uhlén, Simpson, Lundberg: Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells. in Nature methods 2013
The Drosophila proteinin CG8552 is a phosphatidic acid phospholipase A1 and mediates endoplasmic reticulum-Golgi transit of a family of G protein-coupled receptors.
A basic cluster and a hydrophobic interface in the DDHD and SAM (show TTN Antibodies) domains, respectively, are required for p125A-mediated functional endoplasmic reticulum exit site assembly.
Xenopus sec23ip is required for normal neural crest cell development, suggesting a role for the human ortholog in Waardenburg syndrome neural crest defects.
The results suggest that p125A is part of the Sec13 (show SEC13 Antibodies)/Sec31A (show SEC31A Antibodies) subcomplex and facilitates ER export in mammalian cells.
p125 (show XPC Antibodies) is a mammalian-specific component of ER exit sites and participates in the organization of this compartment
These results suggest that p125/Sec23-interacting protein plays an important role in spermiogenesis.
This gene encodes a member of the phosphatidic acid preferring-phospholipase A1 family. The encoded protein is localized to endoplasmic reticulum exit sites and plays a critical role in ER-Golgi transport as part of the multimeric coat protein II complex. An orthologous gene in frogs is required for normal neural crest cell development, suggesting that this gene may play a role in Waardenburg syndrome neural crest defects. Alternatively spliced transcript variants have been observed for this gene.
, SEC23 interacting protein
, Sec23-interacting protein p125
, Sec23-interacting protein
, SEC23-interacting protein-like